JP2781544B2 - 変性シリコアルミノホスフェート分子ふるいを含む触媒を用いる炭素数８の芳香族化合物の異性化方法 - Google Patents
変性シリコアルミノホスフェート分子ふるいを含む触媒を用いる炭素数８の芳香族化合物の異性化方法Info
- Publication number
- JP2781544B2 JP2781544B2 JP8100810A JP10081096A JP2781544B2 JP 2781544 B2 JP2781544 B2 JP 2781544B2 JP 8100810 A JP8100810 A JP 8100810A JP 10081096 A JP10081096 A JP 10081096A JP 2781544 B2 JP2781544 B2 JP 2781544B2
- Authority
- JP
- Japan
- Prior art keywords
- isomerization
- catalyst
- xylene
- molecular sieve
- platinum
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 64
- 238000000034 method Methods 0.000 title claims abstract description 42
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 239000002808 molecular sieve Substances 0.000 title claims abstract description 21
- 150000001491 aromatic compounds Chemical class 0.000 title claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 44
- 238000006317 isomerization reaction Methods 0.000 claims abstract description 40
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 34
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims abstract description 31
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 14
- 230000008569 process Effects 0.000 claims abstract description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 34
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 31
- 229910052751 metal Inorganic materials 0.000 claims description 24
- 239000002184 metal Substances 0.000 claims description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 22
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- 229910052697 platinum Inorganic materials 0.000 claims description 12
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- 229910052809 inorganic oxide Inorganic materials 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 4
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- 125000003118 aryl group Chemical group 0.000 abstract description 8
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- 230000002378 acidificating effect Effects 0.000 abstract description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 23
- 238000006243 chemical reaction Methods 0.000 description 19
- 239000000047 product Substances 0.000 description 12
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- -1 alkyl aromatic hydrocarbon Chemical class 0.000 description 10
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- 239000000463 material Substances 0.000 description 5
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- 238000001179 sorption measurement Methods 0.000 description 5
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- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 4
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- 230000000694 effects Effects 0.000 description 3
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- CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 description 3
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
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- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 2
- VIDOPANCAUPXNH-UHFFFAOYSA-N 1,2,3-triethylbenzene Chemical compound CCC1=CC=CC(CC)=C1CC VIDOPANCAUPXNH-UHFFFAOYSA-N 0.000 description 1
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
- YQZBFMJOASEONC-UHFFFAOYSA-N 1-Methyl-2-propylbenzene Chemical compound CCCC1=CC=CC=C1C YQZBFMJOASEONC-UHFFFAOYSA-N 0.000 description 1
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- DMUVQFCRCMDZPW-UHFFFAOYSA-N 1-ethyl-2-propylbenzene Chemical compound CCCC1=CC=CC=C1CC DMUVQFCRCMDZPW-UHFFFAOYSA-N 0.000 description 1
- VBWYZPGRKYRKNV-UHFFFAOYSA-N 3-propanoyl-1,3-benzoxazol-2-one Chemical compound C1=CC=C2OC(=O)N(C(=O)CC)C2=C1 VBWYZPGRKYRKNV-UHFFFAOYSA-N 0.000 description 1
- ZZBAGJPKGRJIJH-UHFFFAOYSA-N 7h-purine-2-carbaldehyde Chemical compound O=CC1=NC=C2NC=NC2=N1 ZZBAGJPKGRJIJH-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
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- 241000640882 Condea Species 0.000 description 1
- 229910052692 Dysprosium Inorganic materials 0.000 description 1
- 229910015372 FeAl Inorganic materials 0.000 description 1
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229910020068 MgAl Inorganic materials 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- YVDLTVYVLJZLLS-UHFFFAOYSA-J O.Cl[Pt](Cl)(Cl)Cl Chemical compound O.Cl[Pt](Cl)(Cl)Cl YVDLTVYVLJZLLS-UHFFFAOYSA-J 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
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- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000005899 aromatization reaction Methods 0.000 description 1
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- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
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- 238000004523 catalytic cracking Methods 0.000 description 1
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- 238000004517 catalytic hydrocracking Methods 0.000 description 1
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- 229910052757 nitrogen Inorganic materials 0.000 description 1
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- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
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- 241000894007 species Species 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
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- 239000011593 sulfur Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
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- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- CTDPVEAZJVZJKG-UHFFFAOYSA-K trichloroplatinum Chemical compound Cl[Pt](Cl)Cl CTDPVEAZJVZJKG-UHFFFAOYSA-K 0.000 description 1
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
- C07C15/067—C8H10 hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2702—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously
- C07C5/2708—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously with crystalline alumino-silicates, e.g. molecular sieves
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/82—Phosphates
- C07C2529/84—Aluminophosphates containing other elements, e.g. metals, boron
- C07C2529/85—Silicoaluminophosphates (SAPO compounds)
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42736295A | 1995-04-24 | 1995-04-24 | |
| US08/427,362 | 1995-04-24 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH08310977A JPH08310977A (ja) | 1996-11-26 |
| JP2781544B2 true JP2781544B2 (ja) | 1998-07-30 |
Family
ID=23694545
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8100810A Expired - Fee Related JP2781544B2 (ja) | 1995-04-24 | 1996-04-23 | 変性シリコアルミノホスフェート分子ふるいを含む触媒を用いる炭素数８の芳香族化合物の異性化方法 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US5898090A (de) |
| EP (1) | EP0739873B1 (de) |
| JP (1) | JP2781544B2 (de) |
| KR (1) | KR100197926B1 (de) |
| CN (1) | CN1054596C (de) |
| AT (1) | ATE188463T1 (de) |
| AU (1) | AU702788B2 (de) |
| CA (1) | CA2174045C (de) |
| DE (1) | DE69605967T2 (de) |
| DK (1) | DK0739873T3 (de) |
| ES (1) | ES2140786T3 (de) |
| GR (1) | GR3032969T3 (de) |
| MX (1) | MX9601503A (de) |
| MY (1) | MY121583A (de) |
| NO (1) | NO304936B1 (de) |
| PT (1) | PT739873E (de) |
| RO (1) | RO117968B1 (de) |
| RU (1) | RU2125977C1 (de) |
| SG (1) | SG43354A1 (de) |
| TW (1) | TW324713B (de) |
| ZA (1) | ZA963008B (de) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1044615C (zh) * | 1997-03-26 | 1999-08-11 | 熊斌 | 一种代替乙炔气的液化烃类燃气 |
| US6383967B1 (en) * | 1997-12-08 | 2002-05-07 | Uop Llc | Selective aromatics disproportionation/transalkylation catalyst |
| US6222086B1 (en) | 1999-07-02 | 2001-04-24 | Uop Llc | Aromatics isomerization using a dual-catalyst system |
| US6512155B1 (en) | 2000-04-25 | 2003-01-28 | Uop Llc | Process for the activation of an alkylaromatic isomerization catalyst by water |
| JP4058619B2 (ja) * | 2001-10-25 | 2008-03-12 | セイコーエプソン株式会社 | 半導体ウエハ |
| US7405177B2 (en) * | 2003-11-07 | 2008-07-29 | Uop Llc | Catalyst for selective opening of cyclic naphtha and process for using the catalyst |
| US7407907B2 (en) * | 2003-11-07 | 2008-08-05 | Uop Llc | Dual functional catalyst for selective opening of cyclic paraffins and process for using the catalyst |
| US20050101474A1 (en) * | 2003-11-07 | 2005-05-12 | Galperin Leonid B. | Catalyst for selective opening of cyclic naphtha and process for using the catalyst |
| US20060281957A1 (en) * | 2003-11-07 | 2006-12-14 | Galperin Leonid B | Dual functional catalyst for selective opening of cyclic paraffins and process for using the catalyst |
| US20050101819A1 (en) * | 2003-11-07 | 2005-05-12 | Galperin Leonid B. | Dual functional catalyst for selective opening of cyclic paraffins and process for using the catalyst |
| JP4939947B2 (ja) * | 2003-12-30 | 2012-05-30 | ユーオーピー エルエルシー | Ｃ８アルキル芳香族化合物異性化のための方法及び触媒 |
| US20050143615A1 (en) * | 2003-12-30 | 2005-06-30 | Bogdan Paula L. | Process and bimetallic catalyst for C8 alkylaromatic isomerization |
| US20050143614A1 (en) * | 2003-12-30 | 2005-06-30 | Leon-Escamilla E. A. | Process and catalyst for C8 alkylaromatic isomerization |
| CN1325159C (zh) * | 2004-03-22 | 2007-07-11 | 四川大学 | 一种硝基苯选择加氢重排制对氨基苯酚的催化剂 |
| US20070287871A1 (en) * | 2006-03-20 | 2007-12-13 | Eelko Brevoord | Silicoaluminophosphate isomerization catalyst |
| MY153671A (en) * | 2006-03-29 | 2015-03-13 | Toray Industries | Method for conversion of eithylbenzene and process for production of para-xylene |
| CA2762660C (en) | 2009-06-12 | 2017-11-28 | Albemarle Europe Sprl | Sapo molecular sieve catalysts and their preparation and uses |
| US8058496B2 (en) * | 2010-03-31 | 2011-11-15 | Uop Llc | Process for xylene and ethylbenzene isomerization using UZM-35 |
| US8889940B2 (en) * | 2011-11-01 | 2014-11-18 | Uop Llc | Catalyst and process for hydrocarbon conversion |
| US9309170B2 (en) * | 2011-11-14 | 2016-04-12 | Uop Llc | Aromatics isomerization using a dual-catalyst system |
| EP2993163B1 (de) * | 2014-09-05 | 2018-02-21 | Scg Chemicals Co. Ltd. | Verfahren zur Trennung von Ethylbenzol |
| CN110088068B (zh) | 2016-12-21 | 2022-12-06 | 环球油品有限责任公司 | 沸石uzm-55的物质组合物和结构及在芳族分子异构化中的用途 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4943424A (en) | 1988-02-12 | 1990-07-24 | Chevron Research Company | Synthesis of a crystalline silicoaluminophosphate |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4440871A (en) * | 1982-07-26 | 1984-04-03 | Union Carbide Corporation | Crystalline silicoaluminophosphates |
| US4793984A (en) * | 1984-04-13 | 1988-12-27 | Union Carbide Corporation | Molecular sieve compositions |
| US4740650A (en) * | 1986-06-16 | 1988-04-26 | Union Carbide Corporation | Xylene isomerization |
| US5208005A (en) * | 1988-02-12 | 1993-05-04 | Chevron Research And Technology Company | Synthesis of a crystalline silicoaluminophosphate |
| US5158665A (en) * | 1988-02-12 | 1992-10-27 | Chevron Research And Technology Company | Synthesis of a crystalline silicoaluminophosphate |
| US5087347A (en) * | 1988-02-12 | 1992-02-11 | Chevron Research Company | Silicoaluminophosphate hydrocarbon conversion process using SM-3 |
| US5552182A (en) * | 1995-01-31 | 1996-09-03 | Rowland Institute For Science | Inking methods and compositions for production of digitized stereoscopic polarizing images |
-
1996
- 1996-04-12 PT PT96302578T patent/PT739873E/pt unknown
- 1996-04-12 EP EP96302578A patent/EP0739873B1/de not_active Expired - Lifetime
- 1996-04-12 AT AT96302578T patent/ATE188463T1/de not_active IP Right Cessation
- 1996-04-12 DE DE69605967T patent/DE69605967T2/de not_active Expired - Fee Related
- 1996-04-12 ES ES96302578T patent/ES2140786T3/es not_active Expired - Lifetime
- 1996-04-12 CA CA002174045A patent/CA2174045C/en not_active Expired - Fee Related
- 1996-04-12 DK DK96302578T patent/DK0739873T3/da active
- 1996-04-16 ZA ZA963008A patent/ZA963008B/xx unknown
- 1996-04-22 AU AU50780/96A patent/AU702788B2/en not_active Ceased
- 1996-04-22 MX MX9601503A patent/MX9601503A/es not_active IP Right Cessation
- 1996-04-22 MY MYPI96001545A patent/MY121583A/en unknown
- 1996-04-23 CN CN96105444A patent/CN1054596C/zh not_active Expired - Fee Related
- 1996-04-23 JP JP8100810A patent/JP2781544B2/ja not_active Expired - Fee Related
- 1996-04-23 RU RU96107973A patent/RU2125977C1/ru not_active IP Right Cessation
- 1996-04-23 NO NO961613A patent/NO304936B1/no unknown
- 1996-04-23 KR KR1019960012353A patent/KR100197926B1/ko not_active IP Right Cessation
- 1996-04-23 SG SG1996009346A patent/SG43354A1/en unknown
- 1996-04-23 RO RO96-00853A patent/RO117968B1/ro unknown
- 1996-06-04 TW TW085106655A patent/TW324713B/zh active
-
1997
- 1997-12-17 US US08/992,357 patent/US5898090A/en not_active Expired - Fee Related
-
2000
- 2000-03-16 GR GR20000400669T patent/GR3032969T3/el not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4943424A (en) | 1988-02-12 | 1990-07-24 | Chevron Research Company | Synthesis of a crystalline silicoaluminophosphate |
Also Published As
| Publication number | Publication date |
|---|---|
| DK0739873T3 (da) | 2000-05-01 |
| KR960037626A (ko) | 1996-11-19 |
| DE69605967T2 (de) | 2000-10-05 |
| NO304936B1 (no) | 1999-03-08 |
| EP0739873B1 (de) | 2000-01-05 |
| PT739873E (pt) | 2000-06-30 |
| RO117968B1 (ro) | 2002-11-29 |
| ES2140786T3 (es) | 2000-03-01 |
| DE69605967D1 (de) | 2000-02-10 |
| ZA963008B (en) | 1996-11-27 |
| AU702788B2 (en) | 1999-03-04 |
| MX9601503A (es) | 1997-04-30 |
| US5898090A (en) | 1999-04-27 |
| JPH08310977A (ja) | 1996-11-26 |
| MY121583A (en) | 2006-02-28 |
| AU5078096A (en) | 1996-11-07 |
| TW324713B (en) | 1998-01-11 |
| ATE188463T1 (de) | 2000-01-15 |
| CN1054596C (zh) | 2000-07-19 |
| CA2174045C (en) | 2003-01-28 |
| NO961613L (no) | 1996-10-25 |
| NO961613D0 (no) | 1996-04-23 |
| SG43354A1 (en) | 1997-10-17 |
| CN1139659A (zh) | 1997-01-08 |
| KR100197926B1 (ko) | 1999-06-15 |
| CA2174045A1 (en) | 1996-10-25 |
| EP0739873A1 (de) | 1996-10-30 |
| RU2125977C1 (ru) | 1999-02-10 |
| GR3032969T3 (en) | 2000-07-31 |
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